Expanding the spectrum of reactive arthritis (ReA): classic ReA and infection-related arthritis including poststreptococcal ReA, Poncet’s disease, and iBCG-induced ReA
Reactive arthritis (ReA) is a form of sterile arthritis that occurs secondary to an extra-articular infection in genetically predisposed individuals. The extra-articular infection is typically an infection of the gastrointestinal tract or genitourinary tract. Infection-related arthritis is a sterile...
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Veröffentlicht in: | Rheumatology international 2021-08, Vol.41 (8), p.1387-1398 |
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description | Reactive arthritis (ReA) is a form of sterile arthritis that occurs secondary to an extra-articular infection in genetically predisposed individuals. The extra-articular infection is typically an infection of the gastrointestinal tract or genitourinary tract. Infection-related arthritis is a sterile arthritis associated with streptococcal tonsillitis, extra-articular tuberculosis, or intravesical instillation of bacillus Calmette–Guérin (iBCG) therapy for bladder cancer. These infection-related arthritis diagnoses are often grouped with ReA based on the pathogenic mechanism. However, the unique characteristics of these entities may be masked by a group classification. Therefore, we reviewed the clinical characteristics of classic ReA, poststreptococcal ReA, Poncet’s disease, and iBCG-induced ReA. Considering the diversity in triggering microbes, infection sites, and frequency of HLA-B27, these are different disorders. However, the clinical symptoms and intracellular parasitism pathogenic mechanism among classic ReA and infection-related arthritis entities are similar. Therefore, poststreptococcal ReA, Poncet’s disease, and iBCG-induced ReA could be included in the expanding spectrum of ReA, especially based on the pathogenic mechanism. |
doi_str_mv | 10.1007/s00296-021-04879-3 |
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The extra-articular infection is typically an infection of the gastrointestinal tract or genitourinary tract. Infection-related arthritis is a sterile arthritis associated with streptococcal tonsillitis, extra-articular tuberculosis, or intravesical instillation of bacillus Calmette–Guérin (iBCG) therapy for bladder cancer. These infection-related arthritis diagnoses are often grouped with ReA based on the pathogenic mechanism. However, the unique characteristics of these entities may be masked by a group classification. Therefore, we reviewed the clinical characteristics of classic ReA, poststreptococcal ReA, Poncet’s disease, and iBCG-induced ReA. Considering the diversity in triggering microbes, infection sites, and frequency of HLA-B27, these are different disorders. However, the clinical symptoms and intracellular parasitism pathogenic mechanism among classic ReA and infection-related arthritis entities are similar. Therefore, poststreptococcal ReA, Poncet’s disease, and iBCG-induced ReA could be included in the expanding spectrum of ReA, especially based on the pathogenic mechanism.</description><identifier>ISSN: 0172-8172</identifier><identifier>EISSN: 1437-160X</identifier><identifier>DOI: 10.1007/s00296-021-04879-3</identifier><identifier>PMID: 33939015</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Arthritis ; Arthritis, Reactive - etiology ; Arthritis, Reactive - microbiology ; Arthritis, Reactive - physiopathology ; Bladder cancer ; HLA-B27 Antigen ; Humans ; Infections ; Infections - complications ; Medicine ; Medicine & Public Health ; Review ; Rheumatology ; Syndrome</subject><ispartof>Rheumatology international, 2021-08, Vol.41 (8), p.1387-1398</ispartof><rights>The Author(s) 2021</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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Therefore, poststreptococcal ReA, Poncet’s disease, and iBCG-induced ReA could be included in the expanding spectrum of ReA, especially based on the pathogenic mechanism.</description><subject>Arthritis</subject><subject>Arthritis, Reactive - etiology</subject><subject>Arthritis, Reactive - microbiology</subject><subject>Arthritis, Reactive - physiopathology</subject><subject>Bladder cancer</subject><subject>HLA-B27 Antigen</subject><subject>Humans</subject><subject>Infections</subject><subject>Infections - complications</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Review</subject><subject>Rheumatology</subject><subject>Syndrome</subject><issn>0172-8172</issn><issn>1437-160X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kt9qFDEUxoModq2-gBcS8KZCo_kzM5l4IdSlVqGgiIJ3IZs5s5sym4xJpuidr-Ej-Fo-idmdWqsX3iQczu_7Tg75EHrI6FNGqXyWKOWqIZQzQqtWKiJuoQWrhCSsoZ9uowVlkpO2HAfoXkoXtNRNQ--iAyGUUJTVC_Tj9MtofOf8GucN4DSCzXHa4tDjCMZmdwnYxLyJLruEj97DyZPn2A4mJWdxqXARY-f7InPBkwiDydDdkDhvh2nvP4aUU44w5mCDtWbY6Y_xu-At5J_fvifcuQQmwfFs-nJ5RpzvJlv8Cnkf3enNkODB1X2IPr46_bB8Tc7fnr1ZnpwTW1c0k85I1ZiWWm5BSV6zVdtyRSurWLWyEljZu2-44tC1q77uhQG1qhuQvBWyUkwcohez7zitttBZ8DmaQY_RbU38qoNx-u-Odxu9Dpe6pYqpvcHRlUEMnydIWW9dsjAMxkOYkuY1Z5Wq2nqHPv4HvQhT9GW9QlWNbCVTVaH4TNkYUorQXz-GUb1Lgp6ToEsS9D4JWhTRo5trXEt-f30BxAyk0vJriH9m_8f2F_90we8</recordid><startdate>20210801</startdate><enddate>20210801</enddate><creator>Taniguchi, Yoshinori</creator><creator>Nishikawa, Hirofumi</creator><creator>Yoshida, Takeshi</creator><creator>Terada, Yoshio</creator><creator>Tada, Kurisu</creator><creator>Tamura, Naoto</creator><creator>Kobayashi, Shigeto</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2578-5575</orcidid><orcidid>https://orcid.org/0000-0002-1939-3380</orcidid><orcidid>https://orcid.org/0000-0002-8621-7790</orcidid><orcidid>https://orcid.org/0000-0002-0104-8538</orcidid><orcidid>https://orcid.org/0000-0002-6450-1993</orcidid><orcidid>https://orcid.org/0000-0003-1729-2954</orcidid><orcidid>https://orcid.org/0000-0003-3951-4618</orcidid></search><sort><creationdate>20210801</creationdate><title>Expanding the spectrum of reactive arthritis (ReA): classic ReA and infection-related arthritis including poststreptococcal ReA, Poncet’s disease, and iBCG-induced ReA</title><author>Taniguchi, Yoshinori ; 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The extra-articular infection is typically an infection of the gastrointestinal tract or genitourinary tract. Infection-related arthritis is a sterile arthritis associated with streptococcal tonsillitis, extra-articular tuberculosis, or intravesical instillation of bacillus Calmette–Guérin (iBCG) therapy for bladder cancer. These infection-related arthritis diagnoses are often grouped with ReA based on the pathogenic mechanism. However, the unique characteristics of these entities may be masked by a group classification. Therefore, we reviewed the clinical characteristics of classic ReA, poststreptococcal ReA, Poncet’s disease, and iBCG-induced ReA. Considering the diversity in triggering microbes, infection sites, and frequency of HLA-B27, these are different disorders. However, the clinical symptoms and intracellular parasitism pathogenic mechanism among classic ReA and infection-related arthritis entities are similar. Therefore, poststreptococcal ReA, Poncet’s disease, and iBCG-induced ReA could be included in the expanding spectrum of ReA, especially based on the pathogenic mechanism.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>33939015</pmid><doi>10.1007/s00296-021-04879-3</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-2578-5575</orcidid><orcidid>https://orcid.org/0000-0002-1939-3380</orcidid><orcidid>https://orcid.org/0000-0002-8621-7790</orcidid><orcidid>https://orcid.org/0000-0002-0104-8538</orcidid><orcidid>https://orcid.org/0000-0002-6450-1993</orcidid><orcidid>https://orcid.org/0000-0003-1729-2954</orcidid><orcidid>https://orcid.org/0000-0003-3951-4618</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Arthritis Arthritis, Reactive - etiology Arthritis, Reactive - microbiology Arthritis, Reactive - physiopathology Bladder cancer HLA-B27 Antigen Humans Infections Infections - complications Medicine Medicine & Public Health Review Rheumatology Syndrome |
title | Expanding the spectrum of reactive arthritis (ReA): classic ReA and infection-related arthritis including poststreptococcal ReA, Poncet’s disease, and iBCG-induced ReA |
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